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Acidose métabolique
Encéphalopathie métabolique
Maladie métabolique
Maladie métabolique de l'os
Myopathie d'origine métabolique
Syndrome métabolique X
Unité de soins intensifs métaboliques

Translation of "Métabolique " (French → English) :

TERMINOLOGY
see also In-Context Translations below
acidose métabolique

Metabolic acidosis
SNOMEDCT-BE (disorder) / 59455009
SNOMEDCT-BE (disorder) / 59455009


syndrome métabolique X

Dysmetabolic syndrome X
SNOMEDCT-BE (disorder) / 237602007
SNOMEDCT-BE (disorder) / 237602007


maladie métabolique

Metabolic disease
SNOMEDCT-BE (disorder) / 75934005
SNOMEDCT-BE (disorder) / 75934005


maladie métabolique de l'os

Metabolic bone disease
SNOMEDCT-CA (trouble) / 50279003
SNOMEDCT-CA (trouble) / 50279003


les affections endocriniennes et métaboliques transitoires causées par la réponse de l'enfant aux facteurs endocriniens et métaboliques maternels, ou son adaptation à l'existence extra-utérine

transitory endocrine and metabolic disturbances caused by the infant's response to maternal endocrine and metabolic factors, or its adjustment to extrauterine existence
WORLD HEALTH ORGANIZATION ICD-10: P70-P74
WORLD HEALTH ORGANIZATION ICD-10: P70-P74


encéphalopathie métabolique

Metabolic brain syndrome
SNOMEDCT-BE (disorder) / 50122000
SNOMEDCT-BE (disorder) / 50122000


unité de soins intensifs métaboliques

Metabolic ITU
SNOMEDCT-BE (environment) / 309908003
SNOMEDCT-BE (environment) / 309908003


myopathie métabolique par défaut de transport du lactate

A rare metabolic myopathy with characteristics of muscle cramping and/or stiffness after exercise (especially during heat exposure), post-exertional rhabdomyolysis and myoglobinuria and elevation of serum creatine kinase. Caused by mutation in the SL
SNOMEDCT-BE (disorder) / 766715000
SNOMEDCT-BE (especially during heat exposure), post-exertional rhabdomyolysis and myoglobinuria and elevation of serum creatine kinase. Caused by mutation in the SL / 766715000


syndrome de dermatite sévère-allergies multiples-cachexie métabolique

A rare genetic epidermal disorder with characteristics of congenital erythroderma with severe psoriasiform dermatitis, ichthyosis, severe palmoplantar keratoderma, yellow keratosis on the hands and feet, elevated immunoglobulin E, multiple food aller
SNOMEDCT-BE (disorder) / 774211005
SNOMEDCT-BE (disorder) / 774211005


myopathie d'origine métabolique

Metabolic myopathy
SNOMEDCT-BE (disorder) / 26111005
SNOMEDCT-BE (disorder) / 26111005
IN-CONTEXT TRANSLATIONS


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Métabolique

Date index:2023-04-08 -

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